Nascor Pty., Ltd.
AustraliaFDA applicant, unverified
- Devices
- 2
What Nascor Pty., Ltd. makes
Nascor Pty. Ltd. manufactures medical devices including the NASCOR OXYDOME, a device designed for oxygen therapy monitoring, and the NASCOR IGLOO, a portable oxygen delivery system.
These devices are classified as Class I under FDA regulations and are listed in the FDA’s 510(k) registry. The company is based in the United States.
Catalogue
Nascor Oxydome Ref K905627
Regimes: 510(k) Registry: 510(k)Nascor Igloo Ref K935126
Regimes: 510(k) Registry: 510(k)
Frequently asked questions
How many devices does Nascor Pty., Ltd. have in the registry?
The registry currently lists 2 devices for Nascor Pty., Ltd.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Nascor Pty., Ltd.'s devices?
Among its 2 most recently registered devices, Nascor Pty., Ltd. has devices listed in FDA 510(k) (2 devices).
What risk classes do Nascor Pty., Ltd.'s devices fall under?
Among its 2 most recently registered devices, the classes recorded for Nascor Pty., Ltd.'s devices are Class I. Each device page shows its own class and authorisation.
What are the newest devices from Nascor Pty., Ltd. in the registry?
The most recently registered devices listed for Nascor Pty., Ltd. include NASCOR OXYDOME and NASCOR IGLOO.